Validation Results for MinimalCommonOncologyDataElements

Generated Wed Oct 25 23:41:58 UTC 2023, FHIR version 4.0.1 for hl7.fhir.us.mcode#3.0.0 (canonical = http://hl7.org/fhir/us/mcode (history)). See Full QA Report

Quality Checks
Publisher Version:IG Publisher Version: v1.5.0
Publication Code:mcode . PackageId = hl7.fhir.us.mcode, Canonical = http://hl7.org/fhir/us/mcode
Realm Check for US:

Snomed: The IG specifies a different version (http://snomed.info/sct/900000000000207008/version/20230901) to the US edition of SNOMED CT version in the parameters (http://snomed.info/sct/731000124108)

25 Profiles not based on US Core

Publication Request:
package-idhl7.fhir.us.mcode
version3.0.0
pathhttp://hl7.org/fhir/us/mcode/STU3
Pub-Modemilestone
statustrial-use
sequenceSTU 3
descSTU3 Release
descmd

STU3 Release

changeschange_log.html
Proposed path for this milestone publication should usually be canonical with either sequence or version appended
Supressed Messages:66 Suppressed Issues
Dependency Checks:
PackageVersionFHIRCanonicalWeb BaseComment
.. hl7.fhir.us.mcode3.0.0R4http://hl7.org/fhir/us/mcode
... hl7.terminology.r45.3.0 MR4http://terminology.hl7.orghttp://terminology.hl7.org/5.3.0
... hl7.fhir.us.core5.0.1 OR4http://hl7.org/fhir/us/corehttp://hl7.org/fhir/us/core/STU5.0.1Latest Release is 6.1.0
.... hl7.terminology.r43.1.0 OR4http://terminology.hl7.orghttp://terminology.hl7.org/3.1.0Latest Release is 5.3.0
.... hl7.fhir.uv.bulkdata2.0.0 MR4http://hl7.org/fhir/uv/bulkdatahttp://hl7.org/fhir/uv/bulkdata/STU2
.... hl7.fhir.uv.smart-app-launch2.0.0 OR4http://hl7.org/fhir/smart-app-launchhttp://hl7.org/fhir/smart-app-launch/STU2Latest Release is 2.1.0
.... us.nlm.vsac0.7.0 OR4http://fhir.org/packages/us.nlm.vsachttp://fhir.org/packages/us.nlm.vsacLatest Release is 0.13.0
.... hl7.fhir.uv.sdc3.0.0 MR4http://hl7.org/fhir/uv/sdchttp://hl7.org/fhir/uv/sdc/STU3
..... hl7.fhir.r4.examples4.0.1 OR4http://hl7.org/fhirhttp://hl7.org/fhir/R4Latest Release is 5.0.0
... hl7.fhir.uv.genomics-reporting2.0.0 MR4http://hl7.org/fhir/uv/genomics-reportinghttp://hl7.org/fhir/uv/genomics-reporting/STU2
... hl7.fhir.uv.extensions5.1.0-cibuild VR5http://hl7.org/fhir/extensionshttps://build.fhir.org/ig/HL7/fhir-extensions/FHIR Version Mismatch
.... hl7.terminology.r55.3.0 MR5http://terminology.hl7.orghttp://terminology.hl7.org/5.3.0FHIR Version Mismatch
Templates: hl7.fhir.us.mcode.ig-template#0.1.0 -> hl7.fhir.template#current -> hl7.base.template#current -> fhir.base.template#current. Tools: current
Dependent IGs:no references
Global Profiles:(none declared)
HTA Analysis:All OK
R5 Dependencies:(none)
Draft Dependencies:
Modifier Extensions:(none)
Previous Version Comparison:
IPA Comparison: n/a
Summary: errors = 17, warn = 0, info = 0, broken links = 0
FilenameErrorsWarningsHints
Build Errors000
C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Bundle-gx-genomic-bundle-adam-anyperson600
C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Bundle-mcode-patient-bundle-jenny-m100
C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Observation-genomic-variant-fusion100
C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Observation-genomic-variant-germline-deletion100
C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Observation-genomic-variant-jenny-m100
C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Observation-genomic-variant-somatic-single-nucleotide100
C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Observation-gx-genomic-variant-somatic-bap1-indel200
C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Observation-gx-genomic-variant-somatic-pof1b200
C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Observation-gx-genomic-variant-somatic-polrmt200

n/a Show Validation Information


C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Bundle-gx-genomic-bundle-adam-anyperson.json Show Validation Information (208)

PathSeverityMessage
Bundle​.entry[6]​.resource​/*Observation​/gx-genomic-variant-somatic-bap1-indel*​/​.component[2]​.value​.ofType(CodeableConcept) (l405​/c14)errorNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_004656.4:c.1768C>T)
Bundle​.entry[6]​.resource​/*Observation​/gx-genomic-variant-somatic-bap1-indel*​/​.component[3]​.value​.ofType(CodeableConcept) (l424​/c14)errorNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NP_004647.1:p.(Gln590Ter))
Bundle​.entry[12]​.resource​/*Observation​/gx-genomic-variant-somatic-pof1b*​/​.component[4]​.value​.ofType(CodeableConcept) (l1362​/c14)errorNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_001307940.2:c.430C>T)
Bundle​.entry[12]​.resource​/*Observation​/gx-genomic-variant-somatic-pof1b*​/​.component[5]​.value​.ofType(CodeableConcept) (l1381​/c14)errorNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NP_001294869.1:p.(Pro144Ser))
Bundle​.entry[13]​.resource​/*Observation​/gx-genomic-variant-somatic-polrmt*​/​.component[4]​.value​.ofType(CodeableConcept) (l1571​/c14)errorNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_005035.4:c.598G>A)
Bundle​.entry[13]​.resource​/*Observation​/gx-genomic-variant-somatic-polrmt*​/​.component[5]​.value​.ofType(CodeableConcept) (l1590​/c14)errorNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NP_005026.3:p.(Gly200Arg))

C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Bundle-mcode-patient-bundle-jenny-m.json Show Validation Information (110)

PathSeverityMessage
Bundle​.entry[7]​.resource​/*Observation​/genomic-variant-jenny-m*​/​.component[2]​.value​.ofType(CodeableConcept) (l761​/c14)errorNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NC_000016.10:g.23603471G>T)

C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Observation-genomic-variant-fusion.json Show Validation Information (1)

PathSeverityMessage
Observation​.component[2]​.value​.ofType(CodeableConcept) (l75​/c8)errorNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_005157.6(ABL1):c.1076T>G)

C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Observation-genomic-variant-germline-deletion.json Show Validation Information (1)

PathSeverityMessage
Observation​.component[1]​.value​.ofType(CodeableConcept) (l56​/c8)errorNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NG_005905.2:g.126148_126152del)

C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Observation-genomic-variant-jenny-m.json Show Validation Information (9)

PathSeverityMessage
Observation​.component[2]​.value​.ofType(CodeableConcept) (l76​/c8)errorNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NC_000016.10:g.23603471G>T)

C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Observation-genomic-variant-somatic-single-nucleotide.json Show Validation Information (9)

PathSeverityMessage
Observation​.component[2]​.value​.ofType(CodeableConcept) (l75​/c8)errorNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_000455.5:c.725G>A)

C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Observation-gx-genomic-variant-somatic-bap1-indel.json Show Validation Information (10)

PathSeverityMessage
Observation​.component[2]​.value​.ofType(CodeableConcept) (l80​/c8)errorNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_004656.4:c.1768C>T)
Observation​.component[3]​.value​.ofType(CodeableConcept) (l99​/c8)errorNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NP_004647.1:p.(Gln590Ter))

C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Observation-gx-genomic-variant-somatic-pof1b.json Show Validation Information (10)

PathSeverityMessage
Observation​.component[4]​.value​.ofType(CodeableConcept) (l118​/c8)errorNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_001307940.2:c.430C>T)
Observation​.component[5]​.value​.ofType(CodeableConcept) (l137​/c8)errorNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NP_001294869.1:p.(Pro144Ser))

C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Observation-gx-genomic-variant-somatic-polrmt.json Show Validation Information (10)

PathSeverityMessage
Observation​.component[4]​.value​.ofType(CodeableConcept) (l113​/c8)errorNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_005035.4:c.598G>A)
Observation​.component[5]​.value​.ofType(CodeableConcept) (l132​/c8)errorNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NP_005026.3:p.(Gly200Arg))

Suppressed Messages (Warnings, hints, broken links)

DETAILS MESSAGES (THEY APPEAR TO BE FOR GROUPING PURPOSES ONLY)

IG Publisher Spurious Messages

Reference to condition-category code system is inherited from US Core and we can't change that

Reference to deprecated extension included for backwards compatibility.

Reference to work group extension value set containing "CIC" code

SUPPRESS INFORMATION MESSAGES "DOES NOT MATCH ANY KNOWN SLICE" DUE TO TERMINOLOGY LIMITATIONS

SUPPRESS US CORE COMPLIANCE WARNINGS. For STU2, exceptions to US Core parent profiles was approved by Cross-Group Projects Work Group on 1/28/2021 Floyd Eisenberg/Brett Marquard: 28-0-1. See https://jira.hl7.org/browse/FHIR-30707. For STU3, exceptions to US Core parent profiles was approved by the Cross-Group Projects Work Group on 2/9/2023 Saul Kravitz/Floyd Eisenberg: 23-0-2. See https://jira.hl7.org/browse/FHIR-40383. A variance for an additional Observation added in STU3 was approved by the Cross-Group Projects Work Group on 8/10/23. See https://jira.hl7.org/browse/FHIR-41710.

TG263 is a proprietary codesystem used in Radiotherapy. The whole point of conceptmaps is to make it easy to transition to the ValueSets used in this IG. The codesystem identifers TRX, IJE and MRE are not proper codesystem URIs. Work is underway to define proper URIs that will be included in future versions of this IG.

This is a publisher induced issue. The extension in question is introduced by the publisher, not sushi. See https://chat.fhir.org/#narrow/stream/179252-IG-creation/topic/New.20ConceptMap.20Warning.20--.20induced.20by.20IG.20Publisher

UNSUPPORTED TERMINOLOGY

Use of UCUM inherited from Genomics IG (nothing we can do about it)

Value Set Too Large to Validate

Errors sorted by type


Terminology_TX_NoValid_1_CC

C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Bundle-gx-genomic-bundle-adam-anyperson.jsonNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_004656.4:c.1768C>T)
C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Bundle-gx-genomic-bundle-adam-anyperson.jsonNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NP_004647.1:p.(Gln590Ter))
C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Bundle-gx-genomic-bundle-adam-anyperson.jsonNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_001307940.2:c.430C>T)
C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Bundle-gx-genomic-bundle-adam-anyperson.jsonNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NP_001294869.1:p.(Pro144Ser))
C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Bundle-gx-genomic-bundle-adam-anyperson.jsonNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_005035.4:c.598G>A)
C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Bundle-gx-genomic-bundle-adam-anyperson.jsonNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NP_005026.3:p.(Gly200Arg))
C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Bundle-mcode-patient-bundle-jenny-m.jsonNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NC_000016.10:g.23603471G>T)
C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Observation-genomic-variant-fusion.jsonNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_005157.6(ABL1):c.1076T>G)
C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Observation-genomic-variant-germline-deletion.jsonNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NG_005905.2:g.126148_126152del)
C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Observation-genomic-variant-jenny-m.jsonNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NC_000016.10:g.23603471G>T)
C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Observation-genomic-variant-somatic-single-nucleotide.jsonNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_000455.5:c.725G>A)
C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Observation-gx-genomic-variant-somatic-bap1-indel.jsonNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_004656.4:c.1768C>T)
C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Observation-gx-genomic-variant-somatic-bap1-indel.jsonNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NP_004647.1:p.(Gln590Ter))
C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Observation-gx-genomic-variant-somatic-pof1b.jsonNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_001307940.2:c.430C>T)
C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Observation-gx-genomic-variant-somatic-pof1b.jsonNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NP_001294869.1:p.(Pro144Ser))
C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Observation-gx-genomic-variant-somatic-polrmt.jsonNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NM_005035.4:c.598G>A)
C:\temp\hl7.fhir.us.mcode#3.0.0\fsh-generated\resources\Observation-gx-genomic-variant-somatic-polrmt.jsonNone of the codings provided are in the value set 'Human Genome Variation Society (HGVS) Nomenclature' (http://hl7.org/fhir/uv/genomics-reporting/ValueSet/hgvs-vs|2.0.0), and a coding from this value set is required) (codes = http://varnomen.hgvs.org#NP_005026.3:p.(Gly200Arg))